Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.41586474_41586480delCA2637837296KRT14c.356_362del (p.Met119ThrfsTer25)
gnomAD v4
17g.41586474T>ACA399482565KRT14c.361A>T (p.Asn121Tyr)
17g.41586474T>CCA399482567KRT14c.361A>G (p.Asn121Asp)
17g.41586474T>GCA399482564KRT14c.361A>C (p.Asn121His)
17g.41586475C>ACA399482569KRT14c.360G>T (p.Gln120His)
17g.41586475C>GCA399482571KRT14c.360G>C (p.Gln120His)
17g.41586475C>TCA499992006KRT14c.360G>A (p.Gln120=)
17g.41586476T>ACA399482573KRT14c.359A>T (p.Gln120Leu)
17g.41586476T>CCA216907KRT14c.359A>G (p.Gln120Arg)
ClinVar dbSNP
17g.41586476T>GCA216905KRT14c.359A>C (p.Gln120Pro)
ClinVar dbSNP
17g.41586476T=CA2260086839KRT14c.359A= (p.Gln120=)
17g.41586477G>ACA399482580KRT14c.358C>T (p.Gln120Ter)
17g.41586477G>CCA399482578KRT14c.358C>G (p.Gln120Glu)
17g.41586477G>TCA399482576KRT14c.358C>A (p.Gln120Lys)
17g.41586478C>ACA399482581KRT14c.357G>T (p.Met119Ile)
17g.41586478C=CA2260086840KRT14c.357G= (p.Met119=)
17g.41586478C>GCA399482582KRT14c.357G>C (p.Met119Ile)
17g.41586478C>TCA216903KRT14c.357G>A (p.Met119Ile)
ClinVar dbSNP
17g.41586479A=CA2260086841KRT14c.356T= (p.Met119=)
17g.41586479A>CCA399482585KRT14c.356T>G (p.Met119Arg)
ClinVar dbSNP
17g.41586479A>GCA216901KRT14c.356T>C (p.Met119Thr)
ClinVar dbSNP
17g.41586479A>TCA399482586KRT14c.356T>A (p.Met119Lys)
17g.41586480T>ACA399482589KRT14c.355A>T (p.Met119Leu)
17g.41586480T>CCA216899KRT14c.355A>G (p.Met119Val)
ClinVar dbSNP
17g.41586480T>GCA399482590KRT14c.355A>C (p.Met119Leu)
17g.41586480T=CA2260086842KRT14c.355A= (p.Met119=)
17g.41586481G>ACA499992007KRT14c.354C>T (p.Thr118=)
17g.41586481G>CCA499992008KRT14c.354C>G (p.Thr118=)
17g.41586481G=CA2260086843KRT14c.354C= (p.Thr118=)
17g.41586481G>TCA8562735KRT14c.354C>A (p.Thr118=)
dbSNP ExAC gnomAD v3 gnomAD v4
17g.41586482G>ACA16620405KRT14c.353C>T (p.Thr118Ile)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.41586482G>CCA399482594KRT14c.353C>G (p.Thr118Ser)
17g.41586482G=CA2260086844KRT14c.353C= (p.Thr118=)
17g.41586482G>TCA399482596KRT14c.353C>A (p.Thr118Asn)
dbSNP gnomAD v3 gnomAD v4
17g.41586483T>ACA399482599KRT14c.352A>T (p.Thr118Ser)
17g.41586483T>CCA399482600KRT14c.352A>G (p.Thr118Ala)
gnomAD v4
17g.41586483T>GCA399482601KRT14c.352A>C (p.Thr118Pro)
17g.41586484C>ACA8562736KRT14c.351G>T (p.Val117=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586484C=CA2260086845KRT14c.351G= (p.Val117=)
17g.41586484C>GCA499992010KRT14c.351G>C (p.Val117=)
17g.41586484C>TCA499992009KRT14c.351G>A (p.Val117=)
gnomAD v4
17g.41586485A=CA2260086846KRT14c.350T= (p.Val117=)
17g.41586485A>CCA399482604KRT14c.350T>G (p.Val117Gly)
dbSNP
17g.41586485A>GCA399482605KRT14c.350T>C (p.Val117Ala)
dbSNP gnomAD v4
17g.41586485A>TCA399482607KRT14c.350T>A (p.Val117Glu)
17g.41586486C>ACA399482611KRT14c.349G>T (p.Val117Leu)
gnomAD v4
17g.41586486C>GCA399482610KRT14c.349G>C (p.Val117Leu)
17g.41586486C>TCA399482609KRT14c.349G>A (p.Val117Met)
17g.41586487C>ACA399482614KRT14c.348G>T (p.Lys116Asn)
17g.41586487C=CA2260086847KRT14c.348G= (p.Lys116=)
17g.41586487C>GCA216897KRT14c.348G>C (p.Lys116Asn)
ClinVar dbSNP
17g.41586487C>TCA8562737KRT14c.348G>A (p.Lys116=)
dbSNP ExAC gnomAD v2 COSMIC
17g.41586489_41586491delCA2637837297KRT14c.346_348del (p.Lys116del)
gnomAD v4
17g.41586488T>ACA399482619KRT14c.347A>T (p.Lys116Met)
17g.41586488T>CCA399482621KRT14c.347A>G (p.Lys116Arg)
17g.41586488T>GCA399482623KRT14c.347A>C (p.Lys116Thr)
17g.41586489T>ACA216895KRT14c.346A>T (p.Lys116Ter)
ClinVar dbSNP
17g.41586489T>CCA216893KRT14c.346A>G (p.Lys116Glu)
ClinVar dbSNP
17g.41586489T>GCA399482627KRT14c.346A>C (p.Lys116Gln)
gnomAD v4
17g.41586489T=CA2260086848KRT14c.346A= (p.Lys116=)
17g.41586490C>ACA399482630KRT14c.345G>T (p.Glu115Asp)
17g.41586490C>GCA399482631KRT14c.345G>C (p.Glu115Asp)
17g.41586490C>TCA499992011KRT14c.345G>A (p.Glu115=)
17g.41586491T>ACA399482634KRT14c.344A>T (p.Glu115Val)
17g.41586491T>CCA399482636KRT14c.344A>G (p.Glu115Gly)
17g.41586491T>GCA399482637KRT14c.344A>C (p.Glu115Ala)
17g.41586492C>ACA399482644KRT14c.343G>T (p.Glu115Ter)
gnomAD v4
17g.41586492C>GCA399482640KRT14c.343G>C (p.Glu115Gln)
17g.41586492C>TCA399482642KRT14c.343G>A (p.Glu115Lys)
17g.41586493A>CCA399482646KRT14c.342T>G (p.Ser114Arg)
17g.41586493A>GCA499992012KRT14c.342T>C (p.Ser114=)
17g.41586493A>TCA399482648KRT14c.342T>A (p.Ser114Arg)
17g.41586494C>ACA399482650KRT14c.341G>T (p.Ser114Ile)
17g.41586494C>GCA399482652KRT14c.341G>C (p.Ser114Thr)
17g.41586494C>TCA399482654KRT14c.341G>A (p.Ser114Asn)
17g.41586495T>ACA399482655KRT14c.340A>T (p.Ser114Cys)
gnomAD v4
17g.41586495T>CCA399482657KRT14c.340A>G (p.Ser114Gly)
17g.41586495T>GCA8562738KRT14c.340A>C (p.Ser114Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586495T=CA2260086849KRT14c.340A= (p.Ser114=)
17g.41586496G>ACA499992013KRT14c.339C>T (p.Gly113=)
gnomAD v4
17g.41586496G>CCA499992015KRT14c.339C>G (p.Gly113=)
17g.41586496G>TCA499992014KRT14c.339C>A (p.Gly113=)
17g.41586497C>ACA399482661KRT14c.338G>T (p.Gly113Val)
17g.41586497C>GCA399482664KRT14c.338G>C (p.Gly113Ala)
17g.41586497C>TCA399482666KRT14c.338G>A (p.Gly113Asp)
gnomAD v4
17g.41586498C>ACA399482670KRT14c.337G>T (p.Gly113Cys)
17g.41586498C>GCA399482672KRT14c.337G>C (p.Gly113Arg)
17g.41586498C>TCA399482669KRT14c.337G>A (p.Gly113Ser)
17g.41586499C>ACA499992018KRT14c.336G>T (p.Val112=)
17g.41586499C>GCA499992016KRT14c.336G>C (p.Val112=)
17g.41586499C>TCA499992017KRT14c.336G>A (p.Val112=)
17g.41586500A>CCA399482675KRT14c.335T>G (p.Val112Gly)
17g.41586500A>GCA399482676KRT14c.335T>C (p.Val112Ala)
17g.41586500A>TCA399482677KRT14c.335T>A (p.Val112Glu)
17g.41586501C>ACA399482678KRT14c.334G>T (p.Val112Leu)
gnomAD v4
17g.41586501C>GCA399482679KRT14c.334G>C (p.Val112Leu)
17g.41586501C>TCA399482680KRT14c.334G>A (p.Val112Met)
17g.41586502C>ACA499992019KRT14c.333G>T (p.Leu111=)
17g.41586502C>GCA499992020KRT14c.333G>C (p.Leu111=)
17g.41586502C>TCA499992021KRT14c.333G>A (p.Leu111=)
17g.41586503A=CA2260086850KRT14c.332T= (p.Leu111=)
17g.41586503A>CCA399482681KRT14c.332T>G (p.Leu111Arg)
17g.41586503A>GCA399482682KRT14c.332T>C (p.Leu111Pro)
dbSNP
17g.41586503A>TCA399482684KRT14c.332T>A (p.Leu111Gln)
17g.41586504G>ACA499992022KRT14c.331C>T (p.Leu111=)
dbSNP gnomAD v2 gnomAD v4
17g.41586504G>CCA399482686KRT14c.331C>G (p.Leu111Val)
17g.41586504G=CA2260086851KRT14c.331C= (p.Leu111=)
17g.41586504G>TCA399482688KRT14c.331C>A (p.Leu111Met)
17g.41586505A=CA2260086852KRT14c.330T= (p.Leu110=)
17g.41586505A>CCA499992023KRT14c.330T>G (p.Leu110=)
17g.41586505A>GCA8562739KRT14c.330T>C (p.Leu110=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586505A>TCA499992024KRT14c.330T>A (p.Leu110=)
17g.41586510_41586528delCA2809495446KRT14c.312_330del (p.Ala105TrpfsTer7)
17g.41586506A>CCA399482694KRT14c.329T>G (p.Leu110Arg)
17g.41586506A>GCA399482696KRT14c.329T>C (p.Leu110Pro)
17g.41586506A>TCA399482692KRT14c.329T>A (p.Leu110His)
17g.41586507G>ACA399482697KRT14c.328C>T (p.Leu110Phe)
dbSNP gnomAD v2
17g.41586507G>CCA8562740KRT14c.328C>G (p.Leu110Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586507G=CA2260086853KRT14c.328C= (p.Leu110=)
17g.41586507G>TCA399482700KRT14c.328C>A (p.Leu110Ile)
17g.41586508C>ACA499992025KRT14c.327G>T (p.Gly109=)
17g.41586508C=CA2260086854KRT14c.327G= (p.Gly109=)
17g.41586508C>GCA290665625KRT14c.327G>C (p.Gly109=)
dbSNP
17g.41586508C>TCA499992026KRT14c.327G>A (p.Gly109=)
17g.41586509C>ACA399482704KRT14c.326G>T (p.Gly109Val)
17g.41586509C=CA2260086855KRT14c.326G= (p.Gly109=)
17g.41586509C>GCA8562741KRT14c.326G>C (p.Gly109Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586509C>TCA399482703KRT14c.326G>A (p.Gly109Glu)
17g.41586510C>ACA399482707KRT14c.325G>T (p.Gly109Trp)
17g.41586510C>GCA399482709KRT14c.325G>C (p.Gly109Arg)
17g.41586510C>TCA399482711KRT14c.325G>A (p.Gly109Arg)
17g.41586511A=CA2260086856KRT14c.324T= (p.Asp108=)
17g.41586511A>CCA399482713KRT14c.324T>G (p.Asp108Glu)
17g.41586511A>GCA8562743KRT14c.324T>C (p.Asp108=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586511A>TCA8562742KRT14c.324T>A (p.Asp108Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586512T>ACA399482717KRT14c.323A>T (p.Asp108Val)
17g.41586512T>CCA399482722KRT14c.323A>G (p.Asp108Gly)
17g.41586512T>GCA399482720KRT14c.323A>C (p.Asp108Ala)
17g.41586513C>ACA399482724KRT14c.322G>T (p.Asp108Tyr)
17g.41586513C>GCA399482728KRT14c.322G>C (p.Asp108His)
17g.41586513C>TCA399482726KRT14c.322G>A (p.Asp108Asn)
17g.41586514A=CA2260086857KRT14c.321T= (p.Gly107=)
17g.41586514A>CCA499992027KRT14c.321T>G (p.Gly107=)
dbSNP
17g.41586514A>GCA499992028KRT14c.321T>C (p.Gly107=)
17g.41586514A>TCA499992029KRT14c.321T>A (p.Gly107=)
17g.41586515C>ACA399482729KRT14c.320G>T (p.Gly107Val)
17g.41586515C>GCA399482731KRT14c.320G>C (p.Gly107Ala)
17g.41586515C>TCA399482730KRT14c.320G>A (p.Gly107Asp)
gnomAD v4
17g.41586516C>ACA399482733KRT14c.319G>T (p.Gly107Cys)
gnomAD v4
17g.41586516C>GCA399482735KRT14c.319G>C (p.Gly107Arg)
17g.41586516C>TCA399482736KRT14c.319G>A (p.Gly107Ser)
17g.41586517A>CCA499992030KRT14c.318T>G (p.Gly106=)
17g.41586517A>GCA499992031KRT14c.318T>C (p.Gly106=)
17g.41586517A>TCA499992032KRT14c.318T>A (p.Gly106=)
17g.41586518C>ACA399482738KRT14c.317G>T (p.Gly106Val)
17g.41586518C>GCA399482740KRT14c.317G>C (p.Gly106Ala)
dbSNP gnomAD v4
17g.41586518C>TCA399482742KRT14c.317G>A (p.Gly106Asp)
17g.41586519C>ACA399482744KRT14c.316G>T (p.Gly106Cys)
17g.41586519C=CA2260086858KRT14c.316G= (p.Gly106=)
17g.41586519C>GCA399482746KRT14c.316G>C (p.Gly106Arg)
17g.41586519C>TCA399482747KRT14c.316G>A (p.Gly106Ser)
dbSNP gnomAD v4
17g.41586520A>CCA499992033KRT14c.315T>G (p.Ala105=)
17g.41586520A>GCA499992035KRT14c.315T>C (p.Ala105=)
17g.41586520A>TCA499992034KRT14c.315T>A (p.Ala105=)
17g.41586520_41586522delinsAGCCA2260086859KRT14c.313_315delinsGCT (p.Ala105=)
17g.41586521G>ACA399482750KRT14c.314C>T (p.Ala105Val)
17g.41586521G>CCA8562744KRT14c.314C>G (p.Ala105Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586521G=CA2260086861KRT14c.314C= (p.Ala105=)
17g.41586521G>TCA399482753KRT14c.314C>A (p.Ala105Asp)
17g.41586521_41586522delCA216892KRT14c.313_314del (p.Ala105TrpfsTer3)
ClinVar dbSNP
17g.41586521_41586533delinsGCAAAGCCACCACCA2260086860KRT14c.302_314delinsGTGGTGGCTTTGC (p.Gly101=)
17g.41586522C>ACA399482759KRT14c.313G>T (p.Ala105Ser)
17g.41586522C=CA2260086862KRT14c.313G= (p.Ala105=)
17g.41586522C>GCA8562746KRT14c.313G>C (p.Ala105Pro)
dbSNP ExAC gnomAD v2
17g.41586522C>TCA399482758KRT14c.313G>A (p.Ala105Thr)
17g.41586535_41586546delCA8562745KRT14c.302_313del (p.Gly101_Phe104del)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586523A=CA2260086863KRT14c.312T= (p.Phe104=)
17g.41586523A>CCA399482761KRT14c.312T>G (p.Phe104Leu)
17g.41586523A>GCA8562747KRT14c.312T>C (p.Phe104=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
17g.41586523A>TCA399482763KRT14c.312T>A (p.Phe104Leu)
17g.41586524A>CCA399482766KRT14c.311T>G (p.Phe104Cys)
17g.41586524A>GCA399482767KRT14c.311T>C (p.Phe104Ser)
17g.41586524A>TCA399482769KRT14c.311T>A (p.Phe104Tyr)
17g.41586525A>CCA399482772KRT14c.310T>G (p.Phe104Val)
17g.41586525A>GCA399482775KRT14c.310T>C (p.Phe104Leu)
17g.41586525A>TCA399482777KRT14c.310T>A (p.Phe104Ile)
17g.41586526G>ACA8562748KRT14c.309C>T (p.Gly103=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586526G>CCA500205485KRT14c.309C>G (p.Gly103=)
17g.41586526G=CA2260086864KRT14c.309C= (p.Gly103=)
17g.41586526G>TCA500205486KRT14c.309C>A (p.Gly103=)
17g.41586527C>ACA399482781KRT14c.308G>T (p.Gly103Val)
17g.41586527C=CA2260086865KRT14c.308G= (p.Gly103=)
17g.41586527C>GCA399482785KRT14c.308G>C (p.Gly103Ala)
17g.41586527C>TCA399482784KRT14c.308G>A (p.Gly103Asp)
dbSNP
17g.41586528C>ACA399482788KRT14c.307G>T (p.Gly103Cys)
17g.41586528C=CA2260086866KRT14c.307G= (p.Gly103=)
17g.41586528C>GCA399482790KRT14c.307G>C (p.Gly103Arg)
17g.41586528C>TCA8562749KRT14c.307G>A (p.Gly103Ser)
dbSNP ExAC gnomAD v2
17g.41586529A>CCA500205488KRT14c.306T>G (p.Gly102=)
17g.41586529A>GCA500205489KRT14c.306T>C (p.Gly102=)
17g.41586529A>TCA500205491KRT14c.306T>A (p.Gly102=)
17g.41586530C>ACA399482792KRT14c.305G>T (p.Gly102Val)
17g.41586530C=CA2260086867KRT14c.305G= (p.Gly102=)
17g.41586530C>GCA8562750KRT14c.305G>C (p.Gly102Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586530C>TCA399482794KRT14c.305G>A (p.Gly102Asp)
gnomAD v4
17g.41586531C>ACA399482795KRT14c.304G>T (p.Gly102Cys)
17g.41586531C=CA2260086868KRT14c.304G= (p.Gly102=)
17g.41586531C>GCA399482796KRT14c.304G>C (p.Gly102Arg)
dbSNP gnomAD v4
17g.41586531C>TCA399482797KRT14c.304G>A (p.Gly102Ser)
17g.41586532A=CA2260086869KRT14c.303T= (p.Gly101=)
17g.41586532A>CCA8562751KRT14c.303T>G (p.Gly101=)
dbSNP ExAC
17g.41586532A>GCA500205496KRT14c.303T>C (p.Gly101=)
17g.41586532A>TCA500205497KRT14c.303T>A (p.Gly101=)
17g.41586533C>ACA399482799KRT14c.302G>T (p.Gly101Val)
17g.41586533C=CA2260086870KRT14c.302G= (p.Gly101=)
17g.41586533C>GCA8562752KRT14c.302G>C (p.Gly101Ala)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586533C>TCA399482798KRT14c.302G>A (p.Gly101Asp)
17g.41586543_41586590dupCA983759153KRT14c.255_302dup (p.Gly101_Gly102insGlyGlyTyrGlyGlyGlyLeuGlyAlaGlyLeuGlyGlyGlyPheGly)
gnomAD v3 gnomAD v4
17g.41586534C>ACA399482800KRT14c.301G>T (p.Gly101Cys)
17g.41586534C>GCA399482801KRT14c.301G>C (p.Gly101Arg)
17g.41586534C>TCA399482802KRT14c.301G>A (p.Gly101Ser)
17g.41586535A=CA2260086871KRT14c.300T= (p.Phe100=)
17g.41586535A>CCA8562754KRT14c.300T>G (p.Phe100Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586535A>GCA500205499KRT14c.300T>C (p.Phe100=)
17g.41586535A>TCA399482803KRT14c.300T>A (p.Phe100Leu)
17g.41586535_41586547delinsAAAGCCACCACCCCA2260086872KRT14c.288_300delinsGGGTGGTGGCTTT (p.Leu96=)
17g.41586536A>CCA399482804KRT14c.299T>G (p.Phe100Cys)
17g.41586536A>GCA399482805KRT14c.299T>C (p.Phe100Ser)
17g.41586536A>TCA399482806KRT14c.299T>A (p.Phe100Tyr)
17g.41586542_41586553delCA8562753KRT14c.288_299del (p.Leu96_Gly99del)
dbSNP ExAC gnomAD v4
17g.41586537A>CCA399482807KRT14c.298T>G (p.Phe100Val)
17g.41586537A>GCA399482808KRT14c.298T>C (p.Phe100Leu)
17g.41586537A>TCA399482809KRT14c.298T>A (p.Phe100Ile)
17g.41586538G>ACA500205505KRT14c.297C>T (p.Gly99=)
dbSNP gnomAD v3 gnomAD v4
17g.41586538G>CCA500205506KRT14c.297C>G (p.Gly99=)
dbSNP gnomAD v3 gnomAD v4
17g.41586538G=CA2260086873KRT14c.297C= (p.Gly99=)
17g.41586538G>TCA500205507KRT14c.297C>A (p.Gly99=)
17g.41586539C>ACA399482811KRT14c.296G>T (p.Gly99Val)
17g.41586539C>GCA399482812KRT14c.296G>C (p.Gly99Ala)
17g.41586539C>TCA399482810KRT14c.296G>A (p.Gly99Asp)
17g.41586540_41586543delCA2637837315KRT14c.293_296del (p.Gly98AlafsTer19)
gnomAD v4
17g.41586540C>ACA399482815KRT14c.295G>T (p.Gly99Cys)
17g.41586540C=CA2260086874KRT14c.295G= (p.Gly99=)
17g.41586540C>GCA399482813KRT14c.295G>C (p.Gly99Arg)
17g.41586540C>TCA399482814KRT14c.295G>A (p.Gly99Ser)
dbSNP gnomAD v2 gnomAD v4
17g.41586541A=CA2260086875KRT14c.294T= (p.Gly98=)
17g.41586541A>CCA8562755KRT14c.294T>G (p.Gly98=)
dbSNP ExAC gnomAD v4
17g.41586541A>GCA500205512KRT14c.294T>C (p.Gly98=)
17g.41586541A>TCA500205511KRT14c.294T>A (p.Gly98=)
17g.41586542C>ACA399482816KRT14c.293G>T (p.Gly98Val)
COSMIC
17g.41586542C=CA2260086877KRT14c.293G= (p.Gly98=)
17g.41586542C>GCA399482817KRT14c.293G>C (p.Gly98Ala)
dbSNP gnomAD v2 gnomAD v4
17g.41586542C>TCA399482818KRT14c.293G>A (p.Gly98Asp)
dbSNP gnomAD v2 gnomAD v4
17g.41586542_41586554delinsCCACCCAAGCCAGCA2260086876KRT14c.281_293delinsCTGGCTTGGGTGG (p.Ala94=)
17g.41586543C>ACA399482819KRT14c.292G>T (p.Gly98Cys)
17g.41586543C>GCA399482820KRT14c.292G>C (p.Gly98Arg)
17g.41586543C>TCA399482821KRT14c.292G>A (p.Gly98Ser)
gnomAD v4
17g.41586547_41586558delCA772040919KRT14c.281_292del (p.Ala94_Gly97del)
dbSNP gnomAD v3 gnomAD v4
17g.41586544A=CA2260086878KRT14c.291T= (p.Gly97=)
17g.41586544A>CCA8562756KRT14c.291T>G (p.Gly97=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586544A>GCA500205515KRT14c.291T>C (p.Gly97=)
17g.41586544A>TCA500205516KRT14c.291T>A (p.Gly97=)
17g.41586545C>ACA399482822KRT14c.290G>T (p.Gly97Val)
17g.41586545C=CA2260086879KRT14c.290G= (p.Gly97=)
17g.41586545C>GCA399482823KRT14c.290G>C (p.Gly97Ala)
dbSNP
17g.41586545C>TCA399482824KRT14c.290G>A (p.Gly97Asp)
17g.41586546C>ACA399482827KRT14c.289G>T (p.Gly97Cys)
17g.41586546C>GCA399482825KRT14c.289G>C (p.Gly97Arg)
17g.41586546C>TCA399482826KRT14c.289G>A (p.Gly97Ser)
gnomAD v4
17g.41586547C>ACA8562757KRT14c.288G>T (p.Leu96Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586547C=CA2260086880KRT14c.288G= (p.Leu96=)
17g.41586547C>GCA8562758KRT14c.288G>C (p.Leu96Phe)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586547C>TCA500205519KRT14c.288G>A (p.Leu96=)
17g.41586548A>CCA399482828KRT14c.287T>G (p.Leu96Trp)
17g.41586548A>GCA399482829KRT14c.287T>C (p.Leu96Ser)
17g.41586548A>TCA399482830KRT14c.287T>A (p.Leu96Ter)
17g.41586553_41586554insCCACCGAAGCCACA8562759KRT14c.287_288insCGGTGGTGGCTT (p.Gly95_Leu96insPheGlyGlyGly)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586549A>CCA399482831KRT14c.286T>G (p.Leu96Val)
17g.41586549A>GCA500205521KRT14c.286T>C (p.Leu96=)
17g.41586549A>TCA399482832KRT14c.286T>A (p.Leu96Met)
17g.41586550G>ACA500205522KRT14c.285C>T (p.Gly95=)
gnomAD v4
17g.41586550G>CCA500205524KRT14c.285C>G (p.Gly95=)
gnomAD v4
17g.41586550G>TCA500205523KRT14c.285C>A (p.Gly95=)
17g.41586551C>ACA399482833KRT14c.284G>T (p.Gly95Val)
17g.41586551C>GCA399482834KRT14c.284G>C (p.Gly95Ala)
17g.41586551C>TCA399482835KRT14c.284G>A (p.Gly95Asp)
gnomAD v4
17g.41586552C>ACA399482838KRT14c.283G>T (p.Gly95Cys)
17g.41586552C>GCA399482837KRT14c.283G>C (p.Gly95Arg)
17g.41586552C>TCA399482836KRT14c.283G>A (p.Gly95Ser)
COSMIC
17g.41586553A=CA2260086881KRT14c.282T= (p.Ala94=)
17g.41586553A>CCA500205530KRT14c.282T>G (p.Ala94=)
17g.41586553A>GCA500205529KRT14c.282T>C (p.Ala94=)
17g.41586553A>TCA8562760KRT14c.282T>A (p.Ala94=)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586554G>ACA8562761KRT14c.281C>T (p.Ala94Val)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586554G>CCA399482839KRT14c.281C>G (p.Ala94Gly)
dbSNP gnomAD v4
17g.41586554G=CA2260086882KRT14c.281C= (p.Ala94=)
17g.41586554G>TCA399482840KRT14c.281C>A (p.Ala94Asp)
17g.41586555C>ACA399482841KRT14c.280G>T (p.Ala94Ser)
17g.41586555C=CA2260086883KRT14c.280G= (p.Ala94=)
17g.41586555C>GCA399482842KRT14c.280G>C (p.Ala94Pro)
17g.41586555C>TCA216890KRT14c.280G>A (p.Ala94Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586556A>CCA500205532KRT14c.279T>G (p.Gly93=)
17g.41586556A>GCA500205533KRT14c.279T>C (p.Gly93=)
17g.41586556A>TCA500205534KRT14c.279T>A (p.Gly93=)
17g.41586557C>ACA399482843KRT14c.278G>T (p.Gly93Val)
17g.41586557C=CA2260086884KRT14c.278G= (p.Gly93=)
17g.41586557C>GCA399482844KRT14c.278G>C (p.Gly93Ala)
17g.41586557C>TCA399482845KRT14c.278G>A (p.Gly93Asp)
dbSNP gnomAD v4
17g.41586558C>ACA399482846KRT14c.277G>T (p.Gly93Cys)
gnomAD v4
17g.41586558C>GCA399482847KRT14c.277G>C (p.Gly93Arg)
17g.41586558C>TCA399482848KRT14c.277G>A (p.Gly93Ser)
17g.41586559A>CCA500205536KRT14c.276T>G (p.Leu92=)
17g.41586559A>GCA500205537KRT14c.276T>C (p.Leu92=)
gnomAD v4
17g.41586559A>TCA500205538KRT14c.276T>A (p.Leu92=)
17g.41586560A>CCA399482851KRT14c.275T>G (p.Leu92Arg)
17g.41586560A>GCA399482849KRT14c.275T>C (p.Leu92Pro)
17g.41586560A>TCA399482850KRT14c.275T>A (p.Leu92His)
17g.41586561G>ACA399482852KRT14c.274C>T (p.Leu92Phe)
17g.41586561G>CCA399482853KRT14c.274C>G (p.Leu92Val)
17g.41586561G>TCA399482854KRT14c.274C>A (p.Leu92Ile)
17g.41586562G>ACA500205540KRT14c.273C>T (p.Gly91=)
gnomAD v4
17g.41586562G>CCA500205542KRT14c.273C>G (p.Gly91=)
17g.41586562G>TCA500205541KRT14c.273C>A (p.Gly91=)
17g.41586563C>ACA399482855KRT14c.272G>T (p.Gly91Val)
17g.41586563C=CA2260086885KRT14c.272G= (p.Gly91=)
17g.41586563C>GCA399482856KRT14c.272G>C (p.Gly91Ala)
17g.41586563C>TCA399482857KRT14c.272G>A (p.Gly91Asp)
dbSNP gnomAD v3 gnomAD v4
17g.41586564C>ACA399482858KRT14c.271G>T (p.Gly91Cys)
17g.41586564C>GCA399482859KRT14c.271G>C (p.Gly91Arg)
17g.41586564C>TCA399482860KRT14c.271G>A (p.Gly91Ser)
17g.41586565A>CCA500205544KRT14c.270T>G (p.Gly90=)
17g.41586565A>GCA500205545KRT14c.270T>C (p.Gly90=)
17g.41586565A>TCA500205546KRT14c.270T>A (p.Gly90=)
17g.41586566C>ACA399482861KRT14c.269G>T (p.Gly90Val)
17g.41586566C>GCA399482862KRT14c.269G>C (p.Gly90Ala)
17g.41586566C>TCA399482863KRT14c.269G>A (p.Gly90Asp)
17g.41586567C>ACA290665637KRT14c.268G>T (p.Gly90Cys)
dbSNP
17g.41586567C=CA2260086886KRT14c.268G= (p.Gly90=)
17g.41586567C>GCA399482865KRT14c.268G>C (p.Gly90Arg)
17g.41586567C>TCA399482864KRT14c.268G>A (p.Gly90Ser)
17g.41586568A=CA2260086887KRT14c.267T= (p.Gly89=)
17g.41586568A>CCA500205549KRT14c.267T>G (p.Gly89=)
17g.41586568A>GCA500205550KRT14c.267T>C (p.Gly89=)
dbSNP gnomAD v2 gnomAD v4
17g.41586568A>TCA500205551KRT14c.267T>A (p.Gly89=)
17g.41586569C>ACA399482867KRT14c.266G>T (p.Gly89Val)
17g.41586569C=CA2260086888KRT14c.266G= (p.Gly89=)
17g.41586569C>GCA8562762KRT14c.266G>C (p.Gly89Ala)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.41586569C>TCA399482866KRT14c.266G>A (p.Gly89Asp)
dbSNP gnomAD v3 gnomAD v4
17g.41586570C>ACA399482868KRT14c.265G>T (p.Gly89Cys)
17g.41586570C=CA2260086889KRT14c.265G= (p.Gly89=)
17g.41586570C>GCA399482869KRT14c.265G>C (p.Gly89Arg)
17g.41586570C>TCA399482870KRT14c.265G>A (p.Gly89Ser)
dbSNP gnomAD v2 gnomAD v4
17g.41586571A=CA2260086890KRT14c.264T= (p.Tyr88=)
17g.41586571A>CCA399482872KRT14c.264T>G (p.Tyr88Ter)
17g.41586571A>GCA8562763KRT14c.264T>C (p.Tyr88=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.41586571A>TCA399482871KRT14c.264T>A (p.Tyr88Ter)
17g.41586572T>ACA399482873KRT14c.263A>T (p.Tyr88Phe)
17g.41586572T>CCA399482874KRT14c.263A>G (p.Tyr88Cys)
17g.41586572T>GCA399482875KRT14c.263A>C (p.Tyr88Ser)
17g.41586572_41586573delinsTACA2260086891KRT14c.262_263delinsTA (p.Tyr88=)
17g.41586573delCA2260086892KRT14c.262del (p.Tyr88MetfsTer30)
dbSNP
17g.41586573A>CCA399482876KRT14c.262T>G (p.Tyr88Asp)
17g.41586573A>GCA399482877KRT14c.262T>C (p.Tyr88His)
17g.41586573A>TCA399482878KRT14c.262T>A (p.Tyr88Asn)
17g.41586574T>ACA500205558KRT14c.261A>T (p.Gly87=)
dbSNP gnomAD v3 gnomAD v4
17g.41586574T>CCA500205561KRT14c.261A>G (p.Gly87=)
17g.41586574T>GCA500205559KRT14c.261A>C (p.Gly87=)
17g.41586574T=CA2260086893KRT14c.261A= (p.Gly87=)

Number of alleles fetched